Hydroxysteroid sulfotransferase 2B1 affects gastric epithelial function and carcinogenesis induced by a carcinogenic agent
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A healthy gastric mucosal epithelium exhibits tumor-suppressive properties. Gastric epithelial cell dysfunction contributes to gastric cancer development. Oxysterols provided from food or cholesterol oxidation in the gastric epithelium may be further sulfated by hydroxysteroid sulfotransferase 2B1 (SULT2B1), which is highly abundant in the gastric epithelium. However, the effects of SULT2B1 on gastric epithelial function and gastric carcinogenesis are unclear.
A mouse gastric tumor model was established using carcinogenic agent 3-methylcholanthrene (3-MCA). A SULT2B1 deletion (SULT2B1−/−) human gastric epithelial line GES-1 was constructed by CRISPR/CAS9 genome editing system.
The gastric tumor incidence was higher in the SULT2B1−/− mice than in the wild-type (WT) mice. In gastric epithelial cells, adenovirus-mediated SULT2B1b overexpression reduced the levels of oxysterols, such as 24(R/S),25-epoxycholesterol (24(R/S),25-EC) and 27-hydroxycholesterol (27HC). This condition also increased PI3K/AKT signaling to promote gastric epithelial cell proliferation, epithelization, and epithelial development. However, SULT2B1 deletion or SULT2B1 knockdown suppressed PI3K/AKT signaling, epithelial cell epithelization, and wound healing and induced gastric epithelial cell malignant transition upon 3-MCA induction.
The abundant SULT2B1 expression in normal gastric epithelium might maintain epithelial function via the PI3K/AKT signaling pathway and suppress gastric carcinogenesis induced by a carcinogenic agent.
KeywordsGastric epithelial cell Hydroxysteroid Sulfotransferase 2B1 (SULT2B1) Gastric carcinogenesis Oxysterol PI3K/AKT signaling
- 22(R) HC
- 24(S) HC
Epidermal growth factor
Insulin-like growth factor-1
Liquid chromatography and mass spectrometry
Quantitative real-time polymerase chain reaction
Hydroxysteroid Sulfotransferase 2B1
Gastric cancer is the fifth most common cancer worldwide and the second most common cancer in China [1, 2, 3, 4, 5, 6, 7, 8]. Patients with gastric cancer generally have a poor prognosis, with a less than 30% 5-year survival rate in advanced stage . The mechanism underlying gastric carcinogenesis remains to be elucidated.
Gastric mucosal epithelium controls important digestive, absorptive, and secretory functions and forms the first barrier against gastric juice, dietary irritants, and the microbiota. A healthy epithelium is composed of a polarized epithelial cell layer, which is maintained by the integrity of the apical-basal polarity, a highly organized actin cytoskeleton, and a junctional complex exhibiting tumor-suppressive properties . The gastric epithelial cells of the gastric mucosa undergo dynamic changes, such as differentiation, growth, migration, and shedding. Impaired epithelial integrity may contribute to the carcinogenesis of gastric cancer . Growth factors are involved in various aspects of epithelial homeostasis . Epidermal growth factor (EGF) and insulin-like growth factor-1 (IGF-1) participate in the regulation of tight junction (TJ) proteins and wound healing via PI3K/AKT signaling pathway [3, 4, 5, 6, 7, 8].
Oxysterols are derived from dietary or endogenous sources. The majority of endogenous oxysterol species are oxidized derivatives of cholesterol, such as 7α- and 7β-hydroxycholesterol (7αHC, 7βHC), 7-ketocholesterol (7KETO), 4β-hydroxycholesterol (4βHC), 24S-hydroxycholesterol (24(S)HC), 25- hydroxycholesterol (25HC), and 27-hydroxycholesterol (27HC). However, 24 (R/S),25-epoxycholesterol (24(R/S), 25-EC) is formed via a shunt of the mevalonate pathway in parallel to cholesterol synthesis [12, 13, 14, 15, 16]. Oxysterols are not only intermediates in the synthesis of bile acids and steroid hormones but also important regulators of genes involved in cholesterol and lipid metabolism. Oxysterols also may serve important functions in inducing inflammatory responses, cell survival, and differentiation .
In vitro studies, animal studies, and clinical investigations have suggested that oxysterols may play important roles in the pathophysiology of a wide spectrum of diseases, such as cancers and degenerative and age-related diseases. This role is rooted to their ability to trigger cell death, activate oxidation and inflammation, and modulate lipid homeostasis [18, 19, 20, 21]. In addition, oxysterols may decrease the barrier functions of intestinal epithelia and develop an inappropriate inflammatory response to food compounds . Oxysterols have complicated effects on different gastrointestinal cancers. Oxysterols exhibit pro-apoptotic/cytotoxic and pro-cancerous functions in colon tumor cells . Oxysterols cooperate with ROS and lipid peroxides to cause metabolic disorders, DNA damage, and repair disorders; as a result, cell gene mutations that lead to the genesis of cholangiocarcinoma occurs [23, 24, 25]. The levels of 24(R/S),25-EC and 27HC in human gastric tumor tissues are significantly increased compared with those of adjacent normal gastric mucosal tissues. The levels of 24(R/S),25-EC, 25HC, 4βHC, 7αHC, and 7βHC in cancerous gastric juice are dramatically increased compared with gastric juice from healthy subjects .
Hydroxysteroid sulfotransferase 2B1 (SULT2B1) is a member of sulfotransferase that utilizes 3′-phospho-5’adenylyl sulfate as sulfonate donor to catalyze the sulfate conjugation of many hormones, drugs, neurotransmitters, and xenobiotic compounds. SULT2B1a and SULT2B1b, which result from alternative splicing of the SULT2B1 gene, are two isoforms of SULT2B1. SULT2B1b, which is the only SULT2B1 protein detected in human tissues or cell lines, is highly selective for the sulfation of 3β-hydroxysteroids, such as cholesterol, oxysterols, DHEA, D5-adiol, 5a-androstane-3β, 17β-diol (Anstane-diol), and pregnenolone [27, 28, 29]. SULT2B1 is expressed in high level in the stomach. However, the physiological and pathophysiological significance of SULT2B1 in the stomach and the possible role of SULT2B1 in gastric carcinogenesis are poorly understood.
Therefore, the ability of SULT2B1 to modulate oxysterol levels in the gastric epithelium may affect gastric epithelial cell function and gastric carcinogenesis. In the current study, the roles of SULT2B1 and oxysterols on gastric epithelial function were investigated, and the incidence of carcinogenic agent-induced gastric tumor was compared between wild-type (WT) and SULT2B1 deletion (SULT2B1−/−) mice.
Materials and methods
Clinical sample collection
Prior written informed consent was obtained from every patient, and the study was approved by the Ethics Review Board of Fudan University Affiliated Hua’shan Hospital (No. 2017–222). The normal gastric mucosal tissues at various sites (fundus, corpus, and antrum) were collected from 2 gastric cancer patients after total gastrectomy. The tumor tissue and adjacent normal gastric mucosal tissue specimens were collected during radical gastrectomies from 7 patients with gastric adenocarcinoma diagnosed and confirmed by pathological diagnosis and did not receive radiotherapy or chemotherapy. None of these patients was diagnosed with hyperlipidemia or diabetes.
Mouse gastric carcinoma models
All animal experiments were performed with approval from the Fudan University School of Basic Medical Sciences Animal Ethics Committee. The SULT2B1−/− mice were obtained from The Jackson Laboratory (https://www.jax.org/strain/018773). Mouse gastric carcinoma model was established via induction with the carcinogenic agent 3-methylcholanthrene (3-MCA) [30, 31, 32]. Briefly, the WT and SULT2B1−/− mice (age 20–22 weeks) were anesthetized with isoflurane and the stomach was opened along the greater curvature of the anterior wall via laparotomy. A sterile cotton thread with a DMSO-impregnated knot containing approximately 1 mg of 3-MCA was inserted into the lesser curvature of antrum, from mucosa to serosa, through the greater curvature incision. In addition, another knot was tied to the serosal surface so that the two knots riveted the stomach wall. A figure-of-eight suture was carried out to embed the serosal surface knot. Finally, the stomach wall and abdominal incisions were sutured. Twelve weeks after the cotton thread was inserted, the mice were euthanized, and the mouse stomachs and nodules were fixed and processed for histopathological assessment of the cancerous lesions.
The human normal gastric epithelial cell line GES-1 [33, 34, 35] was maintained in RPMI 1640 medium (Invitrogen, CA, USA) supplemented with 10% fetal bovine serum (Gibco, Invitrogen, USA) and 100 units/mL penicillin and streptomycin at 37 °C in a humidified incubator with 5% CO2. Human primary stomach epithelial cells (catalog no. H-6039) were purchased from Cell Biologics Company (IL, USA). The cells were maintained in human epithelial cell medium (catalog no. H6621, Cell Biologics Company).
Infection of GES-1 with adenovirus encoding human SULT2B1b
GES-1 cells were infected with recombinant adenovirus encoding Ad-CMV-SULT2B1b at a multiplicity of infection (MOI) of 20 for 48 h as previously described . The adenovirus encoding Ad-CMV-GFP was used as a control. The recombinant adenoviruses encoding Ad-SULT2B1b were prepared as previously described .
Construction of the SULT2B1−/− GES-1 cell line
To construct the SULT2B1 knockout GES-1 cell line, an online sgRNA design tool based on the clustered, regularly interspaced, short palindromic repeats (CRISPR)/CRISPR-associated protein 9 (CAS9) (CRISPR/CAS9) system (http://crispr.mit.edu/) was utilized. Two sgRNA oligos targeting exon 2 of the SULT2B1 gene were selected as follows: 5′-CGAGTACAGGCCGACGGGGAAGG-3′ (sgRNA-A) and 5′-CGGAGAACACCCAAGATGTGCGG-3′ (sgRNA-B). sgRNA-A and sgRNA-B were cloned into the pSpCas9n (BB)-2A-Puro vector (pX462 vector, Addgene plasmid # 48141) . Then, the constructed plasmids containing sgRNA-A and sgRNA-B were co-transfected into GES-1 cells with Lipofectamine 3000 (Invitrogen, CA, USA). SULT2B1 gene knockout was confirmed by Western blotting and gene sequencing.
siRNA interference and transfection
The cells were transfected with human SULT2B1-specific siRNA duplex oligo ribonucleotides, with a 5′-GATCGAGATCATCTGCTTA-3′ targeting sequence, or negative control duplexes (RiboBio, Guangzhou, China) using Lipofectamine 3000.
cDNA library construction and RNA-seq analysis
Total RNA was extracted with TRIzol (Life Technologies, Thermo Fisher Scientific, USA). A TrueLib mRNA Library Prep Kit for Illumina (ExCell. Bio, Shanghai, China) was adopted for mRNA enrichment and cDNA library preparation. The library quality was assessed using an Agilent 2100 Bioanalyzer. Sequencing was performed on an Illumina HiSeq X Ten at Annoroad Gene Technology Co., Ltd. (Beijing, China).
The data of RNA-seq were analyzed as described previously . The human genome sequence was obtained from the UCSC Genome Browser (GRCh38) (http://genome.ucsc.edu/). The annotated gene models were taken from Ensembl (http://www.ensembl.org/). The RNA-seq reads from the FASTQ files were mapped to the human reference genome (GRCh38), and the splice junctions were identified by TopHat. To estimate transcript abundance, the output files in binary alignment/map (BAM) format were analyzed by Cufflinks. The mRNA abundance was expressed in fragments per kilobase of exon per million reads mapped (FPKM). DAVID (http://david.abcc.ncifcrf.gov/home.jsp) functional annotation cluster analysis was employed to list differentially expressed genes (over 1.5-fold).
Real-time quantitative polymerase chain reaction (qRT-PCR) analysis
Reverse transcription (RT) was performed using a PrimeScript RT reagent kit (Takara, Shiga, Japan) according to the manufacturer’s instructions. The relative expression levels of the target genes were determined by SYBR Premix Ex Taq II (Takara, Shiga, Japan). The tested genes were quantified using the comparative cycle threshold (CT) method, and the results were normalized to the 36B4 level. The primer sets used for gene expression analysis are shown in Table S3.
Western blotting analysis
Samples were lysed in RIPA buffer (Beyotime, Shanghai, China) containing protease inhibitor cocktail, phosphatase inhibitors and phenylmethylsulfonyl fluoride (PMSF). Equal amounts of protein (30–50 μg) were loaded and separated on a 10% SDS-polyacrylamide gel, electrotransferred onto PVDF membranes (Millipore, Billerica, MA, USA), and blocked in 5% bovine serum albumin in Tris-buffered saline containing Tween 20 for 1 h at room temperature. The membranes were probed with primary antibodies against p-AKT (S473), AKT, CCND1, CCNA2, CLND1, CDH1 (Cell Signaling Technology, MA, USA), HSP90 (Proteintech, IL, USA) and SULT2B1 (R&D systems, MN, USA) overnight at 4 °C. After three 10 min washes with Tris-buffered saline with Tween-20 (TBST), the membrane was incubated at room temperature for 1 h with an appropriate secondary antibody conjugated to horseradish peroxidase. HSP90 was used as the loading control. The protein signals were visualized with a Pierce ECL Western Blotting kit (Life Technologies, Thermo Fisher Scientific, USA).
A Cell-Light™ EdU Apollo 567 in vitro kit (RiboBio, Guangzhou, China) was used to determine the proliferative capacity of the cells. The cells (5 × 103) were seeded onto the 96-well microplates and treated as indicated. 5-Ethynyl-2′-deoxyuridine (EdU) was added to the cell culture, and the cells were incubated for 2 h at 37 °C with 5% CO2. Afterwards, the cells were fixed with 4% paraformaldehyde and stained with Hoechst 33342 dye according to the manufacturer’s protocol. Then, the cells were observed under a fluorescence microscope. Cell fluorescence was measured with ImageJ software (National Institutes of Health, MD, USA).
Cells grown on glass coverslips were fixed with 95% ethanol for 20 min at 4 °C and washed 3 × 5 min with PBS. Cells were then blocked in 5% donkey serum/PBS for 30 min and then incubated with rabbit anti-Claudin-1 (Proteintech, IL, USA) in blocking buffer overnight at 4 °C. Cells were then washed 3 × 5 with PBS and then incubated with Alexa Fluor® 594 donkey anti-rabbit IgG. Nuclear DNA was stained by DAPI for 10 min. Cells on the glass coverslips were mounted with antifade mounting medium (Beyotime, Shanghai, China). The fluorescence of the cells was examined by confocal microscopy.
Histopathology and hematoxylin and eosin (H&E) and immunohistochemical staining
After fixation in 4% paraformaldehyde and paraffin embedding, the gastric samples were sliced into 5 mm-thick sections and stained with H&E. Tissue sections were incubated with anti-SULT2B1 (R&D systems, MN, USA), anti-CKpan, anti-CK8, and anti-VIM antibodies (Cell Signaling Technology, MA, USA) and subsequently with a horseradish peroxidase-conjugated secondary antibody. The signals were detected using a diaminobenzidine substrate kit (Vector Laboratories, Burlingame, CA, USA), and the samples were counterstained with hematoxylin. Representative images were captured with a microscope (Leica DFC310 FX).
Wound healing assay
GES-1 or SULT2B1−/− cells were seeded onto the 6-well tissue culture plates. After transfection with Ad-GFP or Ad-SULT2B1b for 6 h, the monolayers were gently scratched with a pipette tip across the center of the well. After the scratch was made, the detached cells were removed by washing. Then the harvested cells were cultured in fresh medium for an additional 48 h. The photos of the same configurations were taken at the indicated times. The gap distance was quantitatively evaluated using ImageJ.
Quantification of oxysterols by liquid chromatography-mass spectrometry (LC-MS)
LC-MS analysis was performed on oxysterols from the same number of pelleted treated cells (1 × 107 cells) using an HPLC-quadrupole time-of-flight hybrid mass system according to the published methods [26, 39]. The typical total ion chromatograms (TIC) of samples are shown in Fig. S1, the multiple reaction monitoring (MRM) condition, quantitation ranges and linearity data are shown in Table S1, the limit of detection (LOD) and limit of quantification (LOQ) data are shown in Table S2.
Experiments were repeated at least three times. Measurable data were expressed as means ± SD. Two-way analysis of variance (ANOVA) was employed to determine statistical differences among time-series experiments while the student’s t-test was performed for two-sample comparisons. The Log-Rank test was used to determine the difference in survival probabilities between the experiment group and the control group. GraphPad Prism 6.0 Software (San Diego, CA, USA) was used for calculations and graphs. P < 0.05 was considered statistically significant.
SULT2B1-deficient mice were susceptible to gastric tumors upon induction with the carcinogenic agent 3-MCA
RNA-seq analysis indicated that SULT2B1 was involved in epithelial development
Global transcriptome profiles between GES-1-Ad-GFP and GES-1-Ad-SULT2B1b groups and between GES-1 and SULT2B1- / - GES-1 groups were compared by RNA sequencing and bioinformatics analysis. GO analysis was performed using DAVID’s default parameters. A total of 481 genes were upregulated and 706 genes were downregulated (over 1.5-fold) in the GES-1-Ad-SULT2B1b group compared with the GES-1-Ad-GFP group. Compared with the GES-1 group, the SULT2B1−/− GES-1 group presented 1068 upregulated genes and 971 downregulated genes (over 1.5-fold change). There are 113 overlapping genes that were upregulated by SULT2B1b overexpression and simultaneously downregulated by SULT2B1 deletion. On KEGG pathway enrichment analysis, the 113 genes were enriched in the “PI3K-AKT signaling pathway” category. Among the genes altered by both SULT2B1b overexpression and SULT2B1 deletion, the genes involved in epithelium development are shown in Fig. 2c heatmap. Key genes, such as CLDN1 and FGF1, that facilitate epithelial development were increased in the Ad-SULT2B1b-treated epithelial cells but decreased in the SULT2B1−/− GES-1 cells. Among the genes that decreased in the Ad-SULT2B1b-treated epithelial cells but increased in the SULT2B1−/− GES-1 cells, BNIPL is involved in epithelial cell proliferation inhibition, and WNT4 and HOXA5 are involved in intestinal epithelial cell development.
SULT2B1b overexpression promoted gastric epithelial cell proliferation via the PI3K/AKT signaling pathway
SULT2B1 deletion suppressed PI3K/AKT signaling and epithelial function in GES-1 cells and contributed to transformation upon 3-MCA induction
Since the SULT2B1−/− mice were susceptible to gastric cancer upon 3-MCA induction, the tumorigenesis transformation tendencies of the GES-1 and SULT2B1−/− GES-1 cells upon 3-MCA (2 μg/m) induction were compared. As shown in Fig. 4f, after 14 days of 3-MCA treatment, compact cell aggregate cultures appeared in the SULT2B1−/− GES-1 cell dish but not in the GES-1 cell dish. After 14 days of 3-MCA induction, the mRNA levels of procancerous genes such as TDGF1, CDX2 and C-Met significantly increased, while the levels of the anticancerous genes RUNX3, P53 and FHIT1 decreased in the SULT2B1−/− GES-1 cells. This change was greater in the SULT2B1−/− cells than in the GES-1 cells (Fig. 4g).
24(R/S),25-EC and 27HC regulate gastric epithelial function
SULT2B1 knockdown and oxysterols suppressed PI3K/AKT signaling in human primary stomach epithelial cells
EGF and IGF-1 promote gastric epithelial cell proliferation, epithelization, wound healing, and epithelial development through the PI3K/AKT signaling pathways. The present study suggests that loss of SULT2B1 expression in normal gastric epithelial cells might suppress gastric epithelial development and promote gastric carcinogenesis upon 3-MCA induction. SULT2B1 might enhance PI3K/AKT signaling and thus promote gastric epithelial cell proliferation, epithelization, and epithelial development.
Hyland PL et al. reported that two SNPs in SULT2B1 (rs4149455 and rs1052131) were associated with esophageal squamous cell carcinoma risk . Previous studies have revealed that SULT2B1b was expressed in hepatocellular carcinoma cells and hepatic progenitor cells but not in normal hepatocytes. The SULT2B1b mRNA levels were higher in clinical hepatocellular carcinoma tumor samples than in samples from the nontumorous tissue adjacent to the tumors [39, 42]. The proliferation-promoting ability of SULT2B1b has also been verified in a partial hepatectomy model .
In vivo and in vitro data have suggested that SULT2B1 deletion contributed to the gastric carcinogenesis induced by the carcinogenic agent 3-MCA. Under physiological conditions, SULT2B1 was nearly exclusively expressed in the gastrointestinal tract, which contained high levels of oxysterols from either food or cholesterol oxidation. For the first time, the relationship between SULT2B1 expression and gastric epithelial function was studied in the present work. The gastric mucosa is continuously exposed to various exogenous and endogenous irritants. Gastric epithelial cell restitution, proliferation, and development are important components of the mucosal defense system. Growth factors, such as EGF and IGF-1, play important roles in adaptive protection by increasing mucosal cell proliferation and enhancing mucosal lesion healing [4, 44, 45]. The present study revealed that SULT2B1 might promote gastric epithelial cell proliferation and wound healing. Claudin-1 is an integral membrane protein and a component of TJ strands, which are located along the cell membrane at the apical edges and are considered critical for epithelial cell polarity . Current data indicates that SULT2B1 deletion or knockdown decreased claudin-1 expression in intracellular compartments, such as cytoplasm and nucleus. The upregulated and intracellular localization of claudin-1 has been reported to be correlated with cell migration and proliferation [47, 48]. The change in the cellular distribution of claudin-1 in gastric epithelial cells affected by SULT2B1 might be a result of differences in cell proliferation between cells transfected with control or SULT2B1-siRNA.
The PI3K/AKT signaling pathway plays essential roles in normal cellular functions, such as protein synthesis, growth control, and nutrition/energy balance. PI3K/AKT activation by growth factors can stimulate protein synthesis and cell growth [49, 50]. The maintenance of gastric epithelial function relies on the proper functioning of the PI3K/AKT pathway. The present data suggested that SULT2B1 deletion inhibited PI3K/AKT signaling in response to growth factors, but SULT2B1 overexpression promoted this pathway. The attenuated response to growth factors might weaken epithelial cell development during the damage-repair process, thereby priming epithelial cells for a malignant transition upon carcinogenic agent induction. Although SULT2B1 might promote normal epithelial cell proliferation via the PI3K/AKT signaling pathway, the PI3K/AKT signaling pathway is still involved in gastric cancer progression. The PI3K/AKT pathway is a frequently activated pathways in gastric cancer, and PI3K inhibitors have been developed to target this prominent signaling cascade . SULT2B1 plays roles in normal gastric epithelial and gastric tumor cells. Chen W et al. reported that SULT2B1 promoted human gastric cancer cell line proliferation and tumor growth in vitro and in vivo . On the basis of the data from The Cancer Genome Atlas, no statistical difference was observed in SULT2B1 mRNA expression between gastric tumor and normal gastric tissue (Fig. S2A) among tumors from patients with stomach adenocarcinoma in different stages (1–4) and grades (1–3) (Fig. S2B, C). SULT2B1 mRNA expressions were higher in gastric tumors from patients with N3, but not N1 or N2 lymph node metastasis, than normal gastric tissue (Fig. S2D). Kaplan–Meier survival analysis indicated that patients with high expression of SULT2B1 in gastric cancer tissue had a lower survival probability than other patients (Fig. S2E). In addition, by immunohistochemical staining, no difference was observed in SULT2B1 expression between gastric cancer and para-tumor tissues from patients with gastric tumor. The representative images are shown in Fig. S2F of the supplemental data. Therefore, the role of SULT2B1 in the development of gastric cancer is complicated and requires further investigation. The present study emphasized the possible role of SULT2B1 in the malignant transformation of normal gastric epithelial cells, that is, gastric carcinogenesis. SULT2B1 might regulate the function of these cells due to the abundant expression of SULT2B1 in normal gastric epithelial cells, thereby promoting their repair after damage and preventing gastric carcinogenesis induced by the carcinogenic agent 3-MCA.
Oxysterols play important functions in regulating lipid and sterol biosynthesis, generating bile acids as substrates and mediating the return of excess cholesterol to the liver for excretion by reverse cholesterol transport . Despite these beneficial effects, oxysterols are also bioactive molecules that induce adverse effects, such as triggering cellular and molecular insults that lead to foam cell formation in the vascular wall and atherogenesis and promoting cytotoxic, oxidative, and/or inflammatory effects involved in many important degenerative diseases . Thus, oxysterols serve protective and cytotoxic functions depending on the different cell types and various cell microenvironments. Oxysterols serve their functions through binding nuclear receptors (e.g., LXR, ROR, and ERα), GPCRs (e.g., GPR183, CXCR2, and SMO), and regulatory or transport proteins (e.g., oxysterol binding protein) . The underlying mechanisms of oxysterols 24(R/S),25-EC and 27-HC regulating PI3K/AKT signaling and gastric epithelial function should be further investigated.
The abundant SULT2B1 expression in the normal gastric epithelium might modulate the oxysterol concentration from food or cholesterol oxidation and regulate epithelial development via the PI3K/AKT signaling pathway. This condition might maintain epithelial function and suppress gastric carcinogenesis induced by carcinogenic agents.
We thank Shanghai Lu-Ming Biotech Co., Ltd. (Shanghai, China) for assistance with Metabonomics analysis.
XB.L. and Q.B. developed the concept and designed the experiments. W.H. and F.G. carried out the experiments and implemented the data analysis. M.Y. and D.X. B.N. helped collecting samples and analysing data. Z.Z. and B.N. participated in discussions of the data. XB.L. and W.H. wrote the manuscript. All authors read and approved the final manuscript.
This work was supported by the National Natural Science Foundation of China (NSFC 31771308 and NSFC 81401939), Shanghai Municipal Commission of Health Natural Science Foundation (No. 20134303), and Shanghai Municipal Natural Science Foundation (17ZR1401800). The funders did not contribute to the study design, data collection, data analysis, decision to publish, or manuscript preparation.
Ethics approval and consent to participate
The study was approved by the Ethics Review Committee of Hua’shan Hospital affiliated to Fudan University (No. 2017–222), and each patient was prior informed. All animal work has been approved from the Fudan University School of Basic Medical Sciences Animal Ethics Committee (No.20160225641064).
Consent for publication
Prior written informed consent was obtained from every patient.
The authors declare no conflict of interest.
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